MEDIMAGING INTEGRATED SOLUTION INC.

FDA Device Registration & Listing · Hsinchu Hsinchu (City), TW · Registration 3015316279

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015316279
FEI Number
3015316279
Entity Name
MEDIMAGING INTEGRATED SOLUTION INC.
City/State/Country
Hsinchu Hsinchu (City), TW
Establishment Address
3F, No.24-2, Industry E. Rd. IV,, Hsinchu Science Park, Hsinchu Hsinchu (City) 30077, TW
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Medimaging Integrated Solution Inc. (Owner Number: 10037829)
Owner / Operator Contact Address
3F, No.24-2, Industry E. Rd. IV, Hsinchu Science Park, Hsinchu, TW-HSZ 30077, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Ophthalmic eye shield MPD 100: MiiS Wound Care System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXQ Reminder, Medication Physical Medicine Class 1 890.5050 2023-10-30
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2022-06-28
HJN Transilluminator, Battery-Powered Ophthalmic Class 1 886.1945 2016-11-29
OUG Medical Device Data System General Hospital Class 1 880.6310 2014-11-01
EOQ Bronchoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4680 2024-08-12
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2024-08-12
FSP Loupe, Diagnostic/Surgical General, Plastic Surgery Class 1 878.4800 2012-02-08
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2012-10-11
HRX Arthroscope Orthopedic Class 2 888.1100 2026-03-18
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2023-11-20
NFG Device, Communications, Images, Ophthalmic Radiology Class 1 892.2020 2021-05-28
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2012-02-08
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 2011-08-23
FTT Camera, Still, Surgical General, Plastic Surgery Class 1 878.4160 2012-07-31
KYT Light, Examination, Medical, Battery Powered General Hospital Class 1 880.6350 2011-08-23
FXN Tape, Camera, Surgical General, Plastic Surgery Class 1 878.4160 2021-03-14
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2022-07-03

Official Correspondent

Luu Hsu

US Agent Details

Ho Shan Wang Email: acmebiotechs@gmail.com Phone: (623) 9864377

Related Public Records

Same Entity

Medimaging Integrated Solution Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K811059 Pentax Precision Instrument Corp. PENTAX BRONCHOFIBERSCOPE #FB-15A 1981-05-27
K142934 Covidien CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved 2015-06-17
K240075 FUJIFILM Healthcare Americas Corporation FUJIFILM Endoscope Model EB-710XT 2024-02-07
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23
K081051 Spine View, Inc. SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE 2008-08-07

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0025-2020 AURIS HEALTH INC 2
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120
Z-0009-2018 Optovue, Inc. 2
iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolution digital imaging device which is suitable for photographing, displaying and storing images of the retina and external areas of the eye to be evaluated under non-mydriatic conditions. The iCam takes digital images of the posterior and external structures of the eye without the use of a mydriatic agent and is intended for use as an aid to clinicians in the evaluation, diagnosis and documentation of ocular health. iCam provides images only and does not provide any diagnostic, pathological analysis or classification of ocular health or disease. AND iVue with Normative Database (K121739) - The iVue is a noncontact, high resolution optical coherence tomography system intended for in vivo imaging, axial cross-sectional, three-dimensional imaging and measurement of anterior and posterior. ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects.
Z-0041-05 Linvatec Corp. 2
Ultra Power Burs, Sterile, Single-Use.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015316279. Last updated year: 2026. Please use registration number 3015316279 when referencing this establishment in official correspondence.
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